143 related articles for article (PubMed ID: 23811035)
1. Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9p.
Bartels I; Pütz I; Reintjes N; Netzer C; Shoukier M
Eur J Med Genet; 2013 Aug; 56(8):458-62. PubMed ID: 23811035
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failure.
Kim MK; Seok HH; Kim YS; Chin MU; Sung SR; Lee WS; Shim SH; Yoon TK
Gene; 2014 Jan; 534(1):54-9. PubMed ID: 24148559
[TBL] [Abstract][Full Text] [Related]
3. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
Kowalczyk M; Tomaszewska A; Podbioł-Palenta A; Constantinou M; Wawrzkiewicz-Witkowska A; Kowalski J; Kałużewski B; Zajączek S; Srebniak MI
Cytogenet Genome Res; 2013; 139(1):9-16. PubMed ID: 22965227
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
[TBL] [Abstract][Full Text] [Related]
5. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
[TBL] [Abstract][Full Text] [Related]
6. Three patients with 9p deletions including DMRT1 and DMRT2: a girl with XY complement, bilateral ovotestes, and extreme growth retardation, and two XX females with normal pubertal development.
Ounap K; Uibo O; Zordania R; Kiho L; Ilus T; Oiglane-Shlik E; Bartsch O
Am J Med Genet A; 2004 Nov; 130A(4):415-23. PubMed ID: 15481033
[TBL] [Abstract][Full Text] [Related]
7. Association of deletion 9p, 46,XY gonadal dysgenesis and autistic spectrum disorder.
Vinci G; Chantot-Bastaraud S; El Houate B; Lortat-Jacob S; Brauner R; McElreavey K
Mol Hum Reprod; 2007 Sep; 13(9):685-9. PubMed ID: 17644778
[TBL] [Abstract][Full Text] [Related]
8. Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis.
Hou QF; Wu D; Chu Y; Liao SX
Taiwan J Obstet Gynecol; 2016 Dec; 55(6):867-870. PubMed ID: 28040136
[TBL] [Abstract][Full Text] [Related]
9. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of a female fetus with ring chromosome 9, 46,XX,r(9)(p24q34), and a de novo interstitial 9p deletion.
Penacho V; Galán F; Martín-Bayón TA; Mayo S; Manchón I; Carrasco A; Martínez-Castellano F; Alcaraz LA
Cytogenet Genome Res; 2014; 144(4):275-9. PubMed ID: 25722017
[TBL] [Abstract][Full Text] [Related]
11. Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype.
Meloni Vde F; Piazzon FB; Soares Mde F; Takeno SS; Christofolini DM; Kulikowski LD; Brunoni D; Melaragno MI
Gene; 2012 Mar; 496(1):59-62. PubMed ID: 22285927
[TBL] [Abstract][Full Text] [Related]
12. Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure.
Harrison SM; Campbell IM; Keays M; Granberg CF; Villanueva C; Tannin G; Zinn AR; Castrillon DH; Shaw CA; Stankiewicz P; Baker LA
Am J Med Genet A; 2013 Oct; 161A(10):2487-94. PubMed ID: 23918653
[TBL] [Abstract][Full Text] [Related]
13. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
[TBL] [Abstract][Full Text] [Related]
14. Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.
Ochalski ME; Engle N; Wakim A; Ravnan BJ; Hoffner L; Rajkovic A; Surti U
Fertil Steril; 2011 Jun; 95(7):2433.e9-15. PubMed ID: 21530964
[TBL] [Abstract][Full Text] [Related]
15. Genitourinary phenotype in XX patients with distal 9p monosomy.
Fujimoto Y; Okuyama T; Iijima M; Tanaka T; Horikawa R; Yamada K; Ogata T
Mol Genet Metab; 2004 Jun; 82(2):173-9. PubMed ID: 15172006
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review.
Chen CP; Su YN; Chen CY; Chern SR; Wu PS; Su JW; Lee CC; Chen LF; Wang W
Genomics; 2013 Oct; 102(4):265-9. PubMed ID: 23981964
[TBL] [Abstract][Full Text] [Related]
17. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
[TBL] [Abstract][Full Text] [Related]
18. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
[TBL] [Abstract][Full Text] [Related]
19. Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure.
Marozzi A; Manfredini E; Tibiletti MG; Furlan D; Villa N; Vegetti W; Crosignani PG; Ginelli E; Meneveri R; Dalprà L
Hum Genet; 2000 Oct; 107(4):304-11. PubMed ID: 11129329
[TBL] [Abstract][Full Text] [Related]
20. An idic(15) associated with POF (premature ovarian failure): molecular cytogenetic definition of a case and review of the literature.
Bertini V; Viola D; Vitti P; Simi P; Valetto A
Gene; 2012 Jul; 503(1):123-5. PubMed ID: 22575723
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
